Ana Salazar Modela Tu Cuerpo Inc. has initiated a nationwide voluntary recall of its Lipofit Extreme Fat Burner 2.0 due to the discovery of undeclared pharmaceutical ingredients. The recall, announced on August 27, 2026, targets Lot 25M12F with an expiration date of September 2027.
FDA laboratory analysis confirmed the presence of fluoxetine, an active ingredient in prescription antidepressants, in the daytime (AM) tablets, and 2,4-dinitrophenol (DNP), a toxic substance not approved for any human use, in the nighttime (PM) tablets. DNP is illegally marketed for weight loss but is commonly used as a pesticide and wood preservative.
Consumption of Lipofit Extreme Fat Burner 2.0, tainted with these substances, poses serious health risks including nausea, vomiting, dizziness, headaches, and potentially fatal cardiac events like rapid heart rate and cardiac arrest. Neurological effects, abnormal bleeding, and suicidal thoughts are also possible. Long-term exposure can lead to damage to vital organs and dangerously high body temperature.
Lipofit Extreme Fat Burner 2.0 is classified as an unapproved new drug, lacking established safety and efficacy. To date, Ana Salazar Modela Tu Cuerpo Inc. has not received any reports of adverse events related to this recall.